Webinar | June 19, 2018

Keeping Your Clinical Trials In Your Hands

Source: Medrio

Whether it’s hiring database programmers or paying your EDC vendor to code your mid-study changes, electronic clinical data management is often dependent upon a whole host of parties outside your organization. But does it have to be this way? In our new on-demand webinar, Charles Gemora, Senior Solutions Engineer at Medrio, looks at how the right EDC system empowers you to conduct your research on your own terms - without relying on the schedule and workflow of external parties. Here’s a snapshot of what you’ll learn:

  • The headaches associated with traditional processes, and how to avoid them
  • How to get your studies built faster - without relying on programming or IT
  • How to make mid-study changes with no downtime

PRESENTED BY CHARLES GEMORA
Senior Solutions Engineer, Medrio

Charles Gemora brings years of experience as an expert in eClinical software solutions to our webinar. He has worked closely with data managers and other professionals across the clinical research industry, from pharma to device and beyond, and has gained an insider perspective on the development of ePRO technology. He holds a Bachelor of Science from University of California, Berkeley, and is currently based in Atlanta, GA.